ADA 1081

ADA 1081

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FDA's Unique Device Identifiction (UDI) Program for Dental Devices and Biologics Regulated as Medical Devices – Technical Report

Published by Publication Date Number of Pages
ADA 02/01/2019 15
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ADA 1081 – FDA's Unique Device Identifiction (UDI) Program for Dental Devices and Biologics Regulated as Medical Devices – Technical Report

ADA 1081-2019: The FDA has issued a rule to establish a system to adequately identify devices through distribution. This rule requires the label of medical devices to include a unique device identifier (UDI), except where the rule provides for an exception or alternative placement.

Product Details

Published:
02/01/2019
Number of Pages:
15
File Size:
1 file , 1.1 MB
Redline File Size:
2 files , 6.3 MB
Note:
This product is unavailable in Ukraine, Russia, Belarus

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